Abstract: The present invention discloses a patient interface having an adaptive system, a respiratory mask and a cushion module adapted with the adaptive system. The adaptive system includes a forehead pressure diffusing portion, a cheek buffering portion and a connecting portion. The forehead pressure diffusing portion is disposed in a frame module. The cheek buffering portion is disposed in a cushion module. The connecting portion is positioned between the forehead pressure diffusing portion and the cheek buffering portion. The connecting portion is configured to transmit pressure between the forehead pressure diffusing portion and the cheek buffering portion. Thus, when a user wears a mask or other devices with the adaptive system, a force received by the face of the user could be automatically and appropriately distributed, further improving comfort of the wearer.

Abstract: The present invention provides a respiratory mask comprising a nose cushion assembly. The nose cushion assembly comprises a base body and a buffering piece. The base body has a base intake portion, a base connection portion, and an air routing piece disposed at the inside of the base body and having a partitioning wall and a wall connection piece. The inside of the partitioning wall encloses an air intake zone. The wall connection piece is disposed outside the partitioning wall and connects with the base intake portion. Between the partitioning wall and the base intake portion there is defined an air outtake zone. The air intake zone is approximately at the center of the base intake portion. The buffering piece connects with the base connection portion and encloses a nose containing room, which in turn connects with the inside of the base body.

Abstract: An air mattress includes a first air cell, a second air cell, a plurality of third air cells, and a body-lifting air cell. The second air cell includes a first air chamber, a second air chamber, and a structurally-weakened region. The body-lifting air cell is below the second air cell and at least one of the third air cells. The body-lifting air cell is inflated by an air source controlled by a control system. When the body-lifting air cell is inflated, a vertical distance between the top of second air cell and the bottom of air mattress is greater than a vertical distance between the top of first air cell and the bottom of air mattress. When the body-lifting air cell is inflated, the second air cell has a lower structural strength than the other air cells to have a cushioning effect against external forces.

Abstract: The present invention discloses a turning air mattress, a turning air cell, and a control method for a turning air mattress. With structural arrangements of an upper portion and a lower portion of the turning air cell as well as inflation and deflation control, the turning air cell having an upper portion that is wider and a lower portion that is narrower can further assist a patient in body turning, enabling the patient to easily achieve a sufficient body turning angle, further reducing the risk of likeliness to pressure sores caused by the structure of the air mattress pressing against the body of the patient.

Abstract: An inflation identification connector and an air mattress system having the same is provided. The inflation identification connector is insertable into a connection seat of a gas delivery host. The connection seat has a light detection component coupled to a controller disposed in the gas delivery host. The inflation identification connector includes a body and an identification structure. The detection result of the light detection component depends on the identification structure and thus is conducive to identification. Upon its insertion into the connection seat, the inflation identification connector is identified by the gas delivery host, enhancing ease of use and protecting manual operation against mistakes. The gas delivery host is not only applicable to different types of air mattresses but also conducive to streamlined management of the air mattress system and reduction of management costs and risks.

Abstract: A patient support structure includes a first supporting part, a second supporting part and a third supporting part. The first supporting part includes a first resilient member; the second supporting part includes a second resilient member; and the third supporting part is between the first supporting part and the second supporting part. The first supporting part, the second supporting part and the third supporting part together define a supporting surface extending along a longitudinal axis, and the second resilient member includes a first supporting area and a second supporting area different in supporting strength.

Abstract: The present disclosure relates to a wound management assembly. The wound management assembly comprises a housing and an exudate collector received in the housing. A gap is defined between the housing and the exudate collector to form a channel for fluid passage, wherein the fluid passes into and through the exudate collector and radially enters the channel.

Abstract: Disclosed is an electromagnetic vibratory pump, comprising a first C-shaped winding and a first magnet. The first C-shaped winding comprises a first coil and a first electromagnetizable member. The first coil covers the first electromagnetizable member, which comprises a first main body, a first leg and a second leg. The legs are connected to the first main body, and the distance between the legs is reduced from a first width to a second width from the first main body. The first magnet swings in a circular tangential direction. A point of tangency of the circular tangential direction is configured apart from the first leg and the second leg respectively by a first minimum distance. The first minimum distance is less than a half of the second width. The first magnet is driven by the first magnetic line of force to move in the first circular tangential direction, and the first magnet is driven by the second magnetic line of force to move in the second circular tangential direction.

Abstract: An inflation and deflation pressure regulation system is applicable to an air mattress with at least two air arrays, the inflation and deflation pressure regulation system comprising an inflation and deflation device, a pressure detection unit and a control unit. The inflation and deflation device inflates or deflates the air mattress; the pressure detection unit continuously detects an instantaneous pressure value of the air mattress; the control unit determines whether the instantaneous pressure value detected by the pressure detection unit when the air mattress is in a weight-bearing state has reached a preset pressure value before a preset time has elapsed, and accordingly uses a first inflation and deflation strategy or a second inflation and deflation strategy to control the inflation and deflation device to inflate or deflate the air mattress.

Abstract: A respiratory mask includes a frame and an elbow engaged with the frame. The frame has a front surface and a rear surface. The front surface defines a connecting hole. The rear surface defines a receiving chamber. The connecting hole is in communication with the receiving chamber. The connecting hole is in communication with the receiving chamber at the rear surface. The elbow has a first end portion. The first end portion is connected with the connecting hole. The first end portion and the frame cooperatively define at least one air flow path communication air in the receiving chamber with external air.

Abstract: A humidifier for a respiratory apparatus includes a first cover, a second cover engaged with the first cover and a partition plate. The first cover defines an air inlet. The second cover defines a chamber configured to contain at least some amount of water. A heater is configured to heat the water to generate humidified air in the chamber. The partition plate is partly sandwiched between the first cover and the second cover. The partition plate defines an air outlet. Air input via the air inlet is humidified by being mixed with the humidified air and thereafter ejected through the air outlet. The air entering via the air inlet is divided by the partition plate into a plurality of flows having different flow velocities, thereby form a plurality of flow paths.

Abstract: A gas communication device comprises a main body, at least one gas delivery pipe and a cover. The gas delivery pipe is at least partially disposed in the main body and forms a gas outlet at one end; the cover is movably pivoted to the main body and comprises at least one sealing structure for correspondingly sealing the gas outlet, wherein the cover is movable along an axis relative to the main body and away from the gas outlet so as to break the seal of the sealing structure on the gas outlet such that the cover is rotatable relative to the main body to expose the gas outlet.

Abstract: An air discharge valve comprises a pipe connection base, a rotary member, at least one seal member and a buffer member. The pipe connection base comprises at least one pipe member which comprises an orifice; the rotary member and the buffer member are both axially connected with the pipe connection base to rotate about a rotation axis relative to the pipe connection base; the rotary member comprises at least one operational part, and the at least one seal member is connected with the rotary member and corresponded to the orifice; the buffer member comprises at least one corresponding operational part, and a rotation buffering space is reserved between each corresponding operational part and each operational part.

Abstract: A negative pressure wound therapy system creates a negative pressure environment in the opening of a wound-dressing unit and a positive pressure environment in the collecting bag. Then a positive pressure detecting procedure is proceeded in the positive pressure environment and a negative pressure detecting procedure is proceeded in the negative pressure environment. The detecting results are sent to determine whether a micro pump is stopped.

Abstract: A wound drainage therapy system includes a wound seal unit, a fluid collector unit, a vacuum driving unit and an actuator. The fluid collector unit is detachably connected with the wound seal unit, and the fluid collector unit has a multiple-pipe integration module and a collection bag. The multiple-pipe integration module has a first row connection port group and a second row connection port group. The vacuum driving unit has a vacuum generator. The actuator has a motor, a negative pressure detector and a positive pressure detector, wherein the motor is used to drive the vacuum generator to operate and the motor is detachably connected with the vacuum generator. A connection port of the negative pressure detector and a connection port of the positive pressure detector are detachably connected with another two connection ports of the second row connection port group respectively.

Abstract: Disclosed is a liquid container for gas humidification, which comprises a first storage chamber containing a bottom; and a second storage chamber comprising a top wall, a bottom wall and a side wall connected between the top wall and the bottom wall, the second storage chamber being provided with at least one opening which is above the bottom of the first storage chamber, thereby enabling the liquid in the second storage chamber to flow into the first storage chamber in a unidirectional way. In addition, also disclosed is a liquid storage device.